2.4糖缀合中的CuAAC

A. Agrahari, A. Mishra, V. Tiwari
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引用次数: 0

摘要

铜(I)催化叠氮化物-炔环加成反应(CuAAC)作为一种通用、可靠、模块化的反应策略,在糖科学领域得到了广泛的研究。在此,我们简要概述了CuAAC点击方法,以方便地获取各种简单和复杂的三唑附加碳水化合物的分子结构。糖基化叠氮化物和末端炔的分子间和分子内CuAAC偶联已被广泛应用于标准键合条件下的区域选择性三唑生成反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
2.4 CuAAC in Carbohydrate Conjugation
Copper(I)-catalyzed azide–alkyne cycloaddition reactions (CuAAC), as a versatile, reliable, and modular strategy, have been widely investigated in the area of glycoscience during the last 20 years. Herein, we presented a brief overview of CuAAC click approaches for easy access to diverse simple and complex triazole-appended carbohydrate-containing molecular architectures. Both intermolecular and intramolecular CuAAC conjugation of glycosylated azides and terminal alkynes have been widely employed for the regioselective triazole-forming reaction under standard click conditions.
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